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east with increasing summer rainfall (Cowling 1983a ). Geophytes are common
and diverse with many species endemic to renosterveld (Proches et al. 2006 ).
Diversity patterns are poorly known but high alpha diversity has been reported
in western regions, with lower diversity and less turnover of shrub species in
eastern communities (see Chapter 11 ).
Renosterveld is poorly studied relative to fynbos. The vegetation has been
highly fragmented by agriculture (> 90% transformed in the Cape region) with
the most extensive remnants on steep mountain slopes (Kemper et al. 2000 ).
Large areas of renosterveld, especially in the east, may have been grasslands
with Elytropappus rhinocerotis invading depending on grazing and fire history.
The shrubland has been converted to C 4 grasslands in southern and eastern
examples by frequent burning to promote grazing (Cowling et al. 1986 ). Similar
human-caused type conversion has occurred in parts of the Cape region as well
(Kraaij 2010 ).
The fire ecology of renosterveld is poorly known. The vegetation supports
crown fires at intervals of several decades, with median frequencies longer than
fynbos in the southern Cape (20-30 yrs; Seydack et al. 2007 ). Cape region
renosterveld, unlike many fynbos communities, resembles California sage scrub
in that the fuel is made up of a continuous shrub layer with a discontinuous
graminoid layer, and similar low fuel loads (see Table 2.1 ).
Elytropappus , the dominant shrub, has a finely branched canopy with very small
cupressoid leaves. It accumulates dead branches and is highly flammable. Indeed
the flammable properties of this single species may account for why renosterveld
replaces succulent Karoo vegetation over much of its range - a plausible example
of niche construction by evolution of flammability in a single species (Bond &
Midgley 1995 ; Kerr et al. 1999 ). Elytropappus is usually killed by fires, though
some resprouting populations are known from the eastern parts of its range.
Recruitment is fire stimulated with shade-intolerant seedlings (Levyns 1929 ). As
in fynbos, the large broadleaf shrubs in renosterveld become more prominent in
thicket formations and all are obligate resprouters (Taylor 1978 ). The fire
responses of other shrubs seem to vary along geographic gradients with fire-
stimulated obligate seeders in mountain renosterveld in the Western Cape (e.g.
Aspalathus spp.), but mostly resprouting members of the Asteraceae ( Relhania ,
Pteronia ) in the eastern distribution of the formation.
Many of the associated geophytes in renosterveld have fire-stimulated
flowering but there is no information on whether fire is an obligate cue. Fire
ephemerals also occur and some have smoke-stimulated germination (C.J.
Fotheringham personal communication) suggesting that, in at least part of its
range, renosterveld has fire-dependent elements. Despite its aridity relative to
fynbos, the more mesic stands of renosterveld are prone to invasion by
alien trees, usually conifers and acacias. Local patches of broadleaf forest
dominated by Olea africana and Rhus spp. occur in fire-protected sites, indicat-
ing a potential for shifting to an alternative ecosystem state in the absence of
burning (Boucher & Moll 1981 ).
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